Canonical Allele Identifier: CA1679787801

Gene: TBXT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.166165782C= , CM000668.2:g.166165782C=	GRCh38
NC_000006.11:g.166579270C= , CM000668.1:g.166579270C=	GRCh37
NC_000006.10:g.166499260C=	NCBI36
NG_012135.1:g.7862G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001366285.2:c.530G= MANE Select	NP_001353214.1:p.Gly177=
ENST00000366876.7:c.530G= MANE Select	ENSP00000355841.3:p.Gly177=
NM_001270484.1:c.530G=	NP_001257413.1:p.Gly177=
NM_001270484.2:c.530G=	NP_001257413.1:p.Gly177=
NM_001366285.1:c.530G=	NP_001353214.1:p.Gly177=
NM_001366286.1:c.530G=	NP_001353215.1:p.Gly177=
NM_001366286.2:c.530G=	NP_001353215.1:p.Gly177=
NM_003181.3:c.530G=	NP_003172.1:p.Gly177=
NM_003181.4:c.530G=	NP_003172.1:p.Gly177=
ENST00000296946.6:c.530G=	ENSP00000296946.2:p.Gly177=
ENST00000366871.7:c.530G=	ENSP00000355836.3:p.Gly177=
ENST00000366876.6:c.530G=	ENSP00000355841.2:p.Gly177=
ENST00000461348.2:c.530G=	ENSP00000453512.1:p.Gly177=
XM_011536080.1:c.530G=	XP_011534382.1:p.Gly177=
XM_011536081.1:c.530G=	XP_011534383.1:p.Gly177=